Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce, and market innovative medicines, solutions, and services in more than 110 countries and regions.
We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities that foster an inclusive environment.
From Quality Assurance, we are looking for a Corporate Quality Auditor who will be responsible for performing Corporate Quality audits on companies within the Grifols Industrial group and affiliates. The goal is to evaluate and ensure compliance with Good Manufacturing Practices, Good Distribution Practices, internal procedures, and policies, as well as to detect opportunities for improvement and best practices. Audits will target Bioscience, Diagnostic, and Hospital division manufacturing sites (Pharmaceutical products and Medical Devices) and Grifols Affiliates.
What your responsibilities will be
Collect the documents required to prepare the audits.
Define the Audit agenda.
Prepare the documents associated with the audit, such as checklists and working sheets.
Conduct the Corporate Quality Audits, ensuring the audit plan established in the agenda is accomplished.
Write the Audit Report detailing the activities carried out, identifying risks and opportunities for improvement, in a timely manner.
Classify the findings and write recommendations.
Review corrective and preventive actions derived from the audit.
Support the management of indicators in the area.
Who you areTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
You have a Life Sciences Degree (Pharmacy, Biology, Chemistry, Biotechnology, etc.) or an Engineering Degree (Chemical or Industrial).
You have 3-5 years of experience in GMP within the pharmaceutical/medical devices/sterile products industry. Experience in Audit and/or Validations is highly valuable.
You have a high proven knowledge of GMP.
Your English is advanced.
You are available to travel approximately 30%.
What we offerIt is a brilliant opportunity for you. Grifols fully recognizes that its employees are one of its major assets. We are committed to maintaining an environment that encourages all employees to develop their professional careers in an excellent working environment.
Information about Grifols is available at [website link].
If you are interested in joining our company and have what it takes for such an exciting position, don’t hesitate to apply! We look forward to receiving your application!
We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please inform us when applying. We are here to help.
Grifols is an equal opportunity employer.
Flexibility for U Program:
Hybrid Model & Flexible Schedule:
Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).
Benefits Package & Contract of Employment:
Permanent position
Location:
Sant Cugat del Vallès, Spain
Learn more about Grifols at [website link].
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